54569-5873 Ondansetron

Product NDC:

54569-5873

Brand Name:

Ondansetron

Generic Name:

Ondansetron

ondansetron hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: ONDANSETRON HYDROCHLORIDE

Strength: 8.0

Unit: mg/1

Packages:

Code: 54569-5873-00

Description: 4 TABLET, FILM COATED in 1 BOTTLE (54569-5873-0)

Effective Date: May 4, 2016

Discontinued:

Code: 54569-5873-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (54569-5873-1)

Effective Date: May 4, 2016

Discontinued:

Code: 54569-5873-02

Description: 3 TABLET, FILM COATED in 1 BOTTLE (54569-5873-2)

Effective Date: May 4, 2016

Discontinued:

Code: 54569-5873-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (54569-5873-3)

Effective Date: May 4, 2016

Discontinued:

Code: 54569-5873-04

Description: 6 TABLET, FILM COATED in 1 BOTTLE (54569-5873-4)

Effective Date: May 4, 2016

Discontinued:

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox